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rs10817938

From SNPedia

Orientationplus
Make rs10817938(C;C)
Make rs10817938(C;T)
Make rs10817938(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position97700127
is asnp
is mentioned by
dbSNPrs10817938
ebirs10817938
HLIrs10817938
Exacrs10817938
Varsomers10817938
Maprs10817938
PheGenIrs10817938
hapmaprs10817938
1000 genomesrs10817938
hgdprs10817938
ensemblrs10817938
gopubmedrs10817938
geneviewrs10817938
scholarrs10817938
googlers10817938
pharmgkbrs10817938
gwascentralrs10817938
openSNPrs10817938
23andMers10817938
23andMe allrs10817938
SNP Nexus

SNPshotrs10817938
SNPdbers10817938
MSV3drs10817938
GWAS Ctlgrs10817938
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 26967386] The association of six polymorphisms of five genes involved in three steps of nucleotide excision repair pathways with hepatocellular cancer risk.


[PMID 27622501] A Functional Polymorphism (rs10817938) in the XPA Promoter Region Is Associated with Poor Prognosis of Oral Squamous Cell Carcinoma in a Chinese Han Population.